GxP Computerised Systems Validation Consultant
Intelance Is this your company? Claim it · London (Remote) · Full-time
Description
About Intelance Intelance is an independent technology, AI and cyber assurance firm based in the UK. We help organisations check, govern and improve their technology through enterprise architecture, AI governance, cyber assurance and data governance work. We are building a small panel of senior associates to deliver technology and AI due diligence on company sales and investments. The role You will check whether software used in drug development is validated to GxP standards, as part of technology due diligence for clients who are selling, buying or investing in life sciences technology companies. Pharmaceutical buyers want proof that a platform producing trial and regulatory outputs works reliably, keeps a full audit trail and would stand up to an inspection. You report to an Intelance engagement partner and work alongside our pharma specialist and technology due diligence lead, who bring your findings into the final report. What you will do Review the validation approach, records and evidence for platforms that produce clinical trial and real world evidence outputs. Check audit trails, access controls, electronic records and change control against 21 CFR Part 11 and EU GMP Annex…
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Questions about this job
Where is this GxP Computerised Systems Validation Consultant job located?
The listing places this job in London (Remote).
Who is hiring?
The employer shown on the listing is Intelance.
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The listing does not state a salary. Ask the employer about pay, overtime and payment dates before accepting.
Is it full-time or part-time?
The listing type is Full-time.
When was this job posted?
It was posted on 10 November 2026. Jobs that stay open too long are closed automatically, so apply soon if you are interested.
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